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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877468Generated: October 30, 2026

1,2-Cyclohexanedione → HCID 67378017, compound

https://huagongshe.com/reaction/877468

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-CyclohexanedioneHCID 13006—
Reactant(2,5-Dichlorophenyl)hydrazine monohydrochlorideHCID 3084937—
SolventMethanolHCID 887—
ProductHCID 67378017HCID 6737801798.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

(2,5-Dichlorophenyl)hydrazine hydrochloride (0.3 g, 1.40 mmol) was dissolved in MeOH (3 mL) and 1,2-cyclo hexadione (0.15 g, 1.40 mmol) was added and the mixture heated to 60° C. for 24 h. The reaction mixture was cooled to room temperature and the volatiles were removed in vacuo. The residue was diluted with water, neutralized with NaHCO3 solution and extracted with EtOAc (3×15 mL). The combined organic extracts were concentrated in vacuo to give the crude compound which was purified by silica gel chromatography [EtOAc-hexane (3:17) as eluant] to provide the title compound (0.35 g, 11.8%). 1H NMR (200 MHz, CDCl3, δ in ppm) 8.92 (bs, 1H), 7.26 (d, J=8.2 Hz, 1H), 7.06 (d, J=8.0 Hz, 1H), 3.36 (t, J=6.2 Hz, 2H), 2.69 (t, J=6.0 Hz, 2H), 2.34-2.21 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987319B2
Source datasetuspto-grants-2015_03
ORD IDord-2165e8e3a3f74a0db088aa7960597654
Source noteuspto-grants-2015_03